Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Surgical Equipment

BD Insyte Autoguard IV Catheters Recalled for Needle Retraction Failure

Agency Publication Date: June 23, 2025
Share:
Sign in to monitor this recall

Summary

Becton Dickinson (BD) is recalling approximately 450 units of BD Insyte Autoguard Shielded IV Catheters due to reports that the needle may retract slowly or fail to retract entirely after use. This defect was identified following customer complaints, although no injuries have been reported to date. The recall includes various models including the Autoguard BC Winged, BC Pro Winged, and standard Winged versions distributed to hospitals and medical supply companies globally.

Risk

If the needle fails to retract properly into its safety shield, it remains exposed after being used on a patient. This significantly increases the risk of accidental needlestick injuries for healthcare workers, which can lead to the transmission of serious bloodborne pathogens such as Hepatitis B, Hepatitis C, or HIV.

What You Should Do

  1. This recall affects multiple models of BD Insyte Autoguard Shielded IV Catheters, including catalog (REF) numbers 381423, 382633, 381533, 381433, 382944, 381811, 382544, 381923, and 381434.
  2. Identify if your product is affected by checking the catalog (REF) and lot numbers printed on the device packaging. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled medical devices immediately and quarantine them to prevent further clinical use.
  4. Contact Becton Dickinson (BD) or your medical supply distributor to arrange for the return, replacement, or correction of the affected catheters.
  5. Call the FDA: 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding this medical device recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: BD Insyte Autoguard Shielded IV Catheter
Variants: 22GA X 1.00 IN (0.9 X 25 MM), 35mL/min
Model / REF:
381423
Lot Numbers:
4229661
UDI:
382903814237
Product: BD Insyte Autoguard BC Winged Shielded IV Catheter
Variants: Blood Control Technology, 20GA x 1.00 in (1.1x25 mm), 63 mL/min
Model / REF:
382633
Lot Numbers:
4222721
UDI:
382903826339
Product: BD Insyte Autoguard Winged Shielded IV Catheter
Variants: 20 GA x 1.00 in (1.1 x 25 mm), 65mL/min
Model / REF:
381533
Lot Numbers:
4282452
UDI:
382903815333
Product: BD Insyte Autoguard Shielded IV Catheter
Variants: 20GA x 1.00 in (1.1x25 mm), 65 mL/min
Model / REF:
381433
Lot Numbers:
4290664
UDI:
382903814336
Product: BD Insyte Autoguard BC Pro Winged Shielded IV Catheter
Variants: 18 GA x 1.16 in (1.3 x 30 mm), 95 mL/min
Model / REF:
382944
Lot Numbers:
4298108
UDI:
382903829446
Product: BD Insyte Autoguard BC Pro Winged Shielded IV Catheter
Variants: 18 GA x 1.16 in (1.3 x 30 mm), 95 mL/min
Model / REF:
381811
Lot Numbers:
4208538
UDI:
00382903818112
Product: BD Insyte Autoguard Shielded IV Catheter
Variants: 18 GA x 1.16 in (1.3 x 30 mm), 95 mL/min
Model / REF:
382544
Lot Numbers:
4312025
UDI:
00382903825448
Product: BD Insyte Autoguard Winged Shielded IV Catheter
Variants: 22 GA x 1.00 in (0.9 x 25 mm), 35 mL/min
Model / REF:
381923
Lot Numbers:
4282308
UDI:
382903819232
Product: BD Insyte Autoguard Shielded IV Catheter
Variants: 20 GA x 1.16 in (1.1 x 30 mm), 60 mL/min
Model / REF:
381434
Lot Numbers:
4116814
UDI:
00382903814343

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96865
Status: Active
Manufacturer: Becton Dickinson Infusion Therapy Systems, Inc.
Sold By: Hospitals; Medical Supply Distributors
Manufactured In: United States
Units Affected: 9 products (50; 50; 50 units; 50 units; 50 units; 50 units; 50 units; 50 units; 50 units)
Distributed To: Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.